Variant report

Variant	esv1815028
Chromosome Location	chr8:87166396-87205568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:87179989-87180133	HepG2	liver:	n/a	n/a
2	CEBPB	chr8:87178834-87179334	A549	lung:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
3	CEBPB	chr8:87178963-87179224	A549	lung:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
4	CEBPB	chr8:87196068-87196211	K562	blood:	n/a	chr8:87196117-87196128
5	CEBPB	chr8:87178969-87179150	HepG2	liver:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
6	CEBPB	chr8:87179916-87180199	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:87178864-87179198	HepG2	liver:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
8	CEBPB	chr8:87195401-87195660	K562	blood:	n/a	n/a
9	CEBPB	chr8:87178890-87179255	HepG2	liver:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
10	CEBPB	chr8:87196022-87196224	HepG2	liver:	n/a	chr8:87196117-87196128
11	CTCF	chr8:87197133-87197169	NHEK	skin:	n/a	n/a
12	CTCF	chr8:87197109-87197178	A549	lung:	n/a	n/a
13	CTCF	chr8:87167248-87167335	MCF-7	breast:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
14	CTCF	chr8:87173761-87173795	GM20000	blood:	n/a	n/a
15	CTCF	chr8:87167258-87167345	MCF-7	breast:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
16	CTCF	chr8:87167131-87167370	HepG2	liver:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
17	CTCF	chr8:87167200-87167350	Hela-S3	cervix:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
18	CTCF	chr8:87167220-87167370	WERI-Rb-1	eye:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
19	CTCF	chr8:87167180-87167330	HepG2	liver:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
20	CTCF	chr8:87197407-87197419	GM20000	blood:	n/a	n/a
21	CTCF	chr8:87197103-87197224	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:87167220-87167370	HepG2	liver:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
23	CTCF	chr8:87197113-87197207	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:87169760-87169910	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:87186248-87186285	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr8:87167200-87167350	GM12871	blood:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
27	CTCF	chr8:87197122-87197189	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:87167209-87167331	HepG2	liver:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
29	CTCF	chr8:87201080-87201230	GM12867	blood:	n/a	n/a
30	CTCF	chr8:87167254-87167320	MCF-7	breast:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
31	CTCF	chr8:87167140-87167290	MCF-7	breast:	n/a	chr8:87167277-87167286 chr8:87167273-87167286 chr8:87167271-87167289
32	E2F4	chr8:87178029-87178299	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr8:87188803-87188979	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr8:87189054-87189336	Hela-S3	cervix:	n/a	chr8:87189194-87189203
35	EP300	chr8:87179830-87180195	HepG2	liver:	n/a	n/a
36	EP300	chr8:87189025-87189384	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
37	EP300	chr8:87188804-87189398	SK-N-SH	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
38	EP300	chr8:87188997-87189386	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
39	FOS	chr8:87188217-87188290	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:87187991-87188555	HUVEC	blood vessel:	n/a	n/a
41	FOS	chr8:87188768-87189386	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
42	FOS	chr8:87195507-87195621	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr8:87188908-87189343	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
44	FOS	chr8:87188684-87189378	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
45	FOS	chr8:87188835-87189335	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
46	FOS	chr8:87188778-87189577	HUVEC	blood vessel:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
47	FOSL1	chr8:87188598-87189574	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
48	FOSL1	chr8:87188728-87189476	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
49	FOSL2	chr8:87189033-87189353	A549	lung:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
50	FOSL2	chr8:87188740-87189499	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202

No.	Distal block	Cell Line	Cell type
1	chr8:87121147..87123014-chr8:87175449..87177682,2	MCF-7	breast:
2	chr8:87169329..87173645-chr8:87175969..87178832,5	MCF-7	breast:
3	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:
4	chr8:87187218..87190589-chr8:87353304..87356196,4	MCF-7	breast:
5	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
6	chr8:87144904..87147607-chr8:87176565..87179307,2	MCF-7	breast:
7	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
8	chr8:87188610..87190453-chr8:87196607..87198359,2	MCF-7	breast:
9	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
10	chr8:87140754..87142619-chr8:87176258..87179083,2	MCF-7	breast:
11	chr8:87193009..87195641-chr8:87198363..87201280,2	MCF-7	breast:
12	chr8:87180045..87182369-chr8:87352740..87355498,2	MCF-7	breast:
13	chr8:87175114..87176771-chr8:87353903..87355811,2	MCF-7	breast:
14	chr8:87169329..87173645-chr8:87175969..87178832,5	MCF-7	breast:
15	chr8:87187097..87192513-chr8:87353340..87357451,6	MCF-7	breast:
16	chr8:87188610..87190453-chr8:87196607..87198359,2	MCF-7	breast:
17	chr8:87198044..87200373-chr8:87209574..87213892,4	MCF-7	breast:
18	chr8:87193009..87195641-chr8:87198363..87201280,2	MCF-7	breast:
19	chr8:87167795..87169493-chr8:87353892..87356513,2	MCF-7	breast:
20	chr8:87175555..87177638-chr8:87179061..87180687,2	K562	blood:
21	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
22	chr8:87177733..87179455-chr8:87185682..87188485,3	MCF-7	breast:
23	chr8:87165113..87167523-chr8:87354412..87356761,2	MCF-7	breast:
24	chr8:87196093..87197608-chr8:87352930..87355663,2	MCF-7	breast:
25	chr8:87202647..87205379-chr8:87353769..87356042,2	MCF-7	breast:
26	chr4:103729408..103730314-chr8:87178649..87179164,2	MCF-7	breast:
27	chr8:87169494..87171967-chr8:87353783..87356273,2	MCF-7	breast:
28	chr8:87177733..87179455-chr8:87185682..87188485,3	MCF-7	breast:
29	chr8:87175555..87177638-chr8:87179061..87180687,2	K562	blood:
30	chr8:87193443..87195770-chr8:87354919..87356635,3	MCF-7	breast:
31	chr8:87192734..87196437-chr8:87354857..87357737,4	MCF-7	breast:
32	chr8:87159431..87162272-chr8:87167025..87170194,3	MCF-7	breast:
33	chr8:87186847..87188623-chr8:87190111..87192908,2	MCF-7	breast:
34	chr8:87180089..87182207-chr8:87303826..87306523,2	MCF-7	breast:
35	chr8:87163948..87165822-chr8:87168496..87170737,2	MCF-7	breast:
36	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
37	chr8:87194628..87197311-chr8:87229703..87231831,2	MCF-7	breast:
38	chr8:87194678..87197306-chr8:87210652..87213144,4	MCF-7	breast:
39	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-1	chr8:87198876-87198935	ENSG00000253699.1
2	lnc-SLC7A13-2	chr8:87166297-87166454	ENSG00000253675.1
3	lnc-SLC7A13-2	chr8:87166252-87166435	ENSG00000253675.1
4	lnc-ATP6V0D2-1	chr8:87192647-87192848	ENSG00000253699.1

Variant related genes	Relation type
ENSG00000253675	TF binding region
ENSG00000253699	TF binding region
ENSG00000253699	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000254231	chromatin interactions

Extended variants
information (count: 1388 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1388 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6983781	chr8:87166396-87166397	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560600862	chr8:87166473-87166474	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145974620	chr8:87166506-87166507	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs183915153	chr8:87166521-87166522	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562744097	chr8:87166570-87166571	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs138513853	chr8:87166578-87166579	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548204047	chr8:87166601-87166602	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs141534886	chr8:87166650-87166651	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566097375	chr8:87166659-87166660	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs55959135	chr8:87166699-87166700	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527513066	chr8:87166706-87166707	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188304751	chr8:87166731-87166732	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576330996	chr8:87166744-87166745	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144368268	chr8:87166758-87166759	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs192702557	chr8:87166822-87166823	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs534104414	chr8:87166962-87166963	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555681045	chr8:87166983-87166984	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs35581784	chr8:87167027-87167028	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200216675	chr8:87167028-87167029	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs556081440	chr8:87167082-87167083	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs148807953	chr8:87167084-87167085	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs569564556	chr8:87167099-87167100	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs13263240	chr8:87167119-87167120	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs554990139	chr8:87167143-87167144	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs575068850	chr8:87167147-87167148	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs540869427	chr8:87167148-87167149	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs554303754	chr8:87167154-87167155	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs577365534	chr8:87167160-87167161	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs185579238	chr8:87167174-87167175	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs10504821	chr8:87167184-87167185	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563853205	chr8:87167230-87167231	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs542088486	chr8:87167244-87167245	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs561683917	chr8:87167251-87167252	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs527477965	chr8:87167259-87167260	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs372408773	chr8:87167279-87167280	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs547239012	chr8:87167314-87167315	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570319923	chr8:87167318-87167319	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs534040136	chr8:87167392-87167393	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549630990	chr8:87167393-87167394	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs142401424	chr8:87167398-87167399	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs535137694	chr8:87167402-87167403	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548852849	chr8:87167406-87167407	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs568817570	chr8:87167422-87167423	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs534498802	chr8:87167424-87167425	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs111665834	chr8:87167489-87167490	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs577528749	chr8:87167505-87167506	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs74323915	chr8:87167546-87167547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556411550	chr8:87167559-87167560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10956172	chr8:87167753-87167754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576371727	chr8:87167766-87167767	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	22341455	CNVD
Rett syndrome	21593744	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87165000-87168600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:87177200-87180000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:87178400-87179000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:87178800-87180000	Enhancers	HepG2	liver
5	chr8:87179800-87180000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:87180000-87185400	Weak transcription	HepG2	liver
7	chr8:87180000-87187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:87185400-87186000	Enhancers	HepG2	liver
9	chr8:87185800-87186200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:87186000-87186200	Flanking Active TSS	HepG2	liver
11	chr8:87186000-87186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:87186000-87186400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr8:87186000-87186400	Enhancers	Gastric	stomach
14	chr8:87186000-87186600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:87186000-87186800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:87186200-87186400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr8:87186200-87188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr8:87186200-87189200	Enhancers	HepG2	liver
19	chr8:87186400-87186600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:87186400-87187400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:87186600-87186800	Enhancers	A549	lung
22	chr8:87186600-87187200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:87186600-87188400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:87186800-87187800	Weak transcription	A549	lung
25	chr8:87186800-87188400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
27	chr8:87187200-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:87187400-87187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:87187400-87188000	Enhancers	HUVEC	blood vessel
30	chr8:87187400-87188200	Enhancers	HMEC	breast
31	chr8:87187400-87188400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:87187600-87188200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr8:87187600-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:87187600-87188200	Enhancers	NHEK	skin
35	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
36	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr8:87187800-87188000	Enhancers	A549	lung
38	chr8:87187800-87188000	Enhancers	HSMMtube	muscle
39	chr8:87187800-87188000	Enhancers	NH-A	brain
40	chr8:87187800-87188200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:87187800-87188400	Enhancers	HSMM	muscle
42	chr8:87187800-87189400	Enhancers	Osteobl	bone
43	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:87188000-87188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:87188000-87188400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:87188000-87188400	Flanking Active TSS	HSMMtube	muscle
47	chr8:87188000-87188600	Enhancers	Fetal Brain Female	brain
48	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:87188000-87189200	Flanking Active TSS	A549	lung

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